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31.
花岗岩类某些矿物中微量元素和挥发分离子探针[SIMS]研究   总被引:1,自引:0,他引:1  
本文采用离子探针(SIMS)分析花岗岩类磷灰石、锆石和黑云母等矿物中微量元素和挥发分,来探讨花岗岩类成矿作用。结果证明,不同时代和不同成因的磷灰石和锆石具有某些指纹特征;并显示了花岗岩类所含微量元素和挥发分之间存在某种相关关系。  相似文献   
32.
Fluid-saturated experiments were conducted to investigate the partitioning of boron among haplogranitic melt, aqueous vapor and brine at 800 °C and 100 MPa. Experiments were carried out in cold-seal pressure vessels for 1 to 21 days, and utilized powdered synthetic subaluminous haplogranite glass doped with 1000 ppm B (crystalline H3BO3) and variable amounts of NaCl and H2O at a fluid/haplogranite mass RATIO=1:1. Run-product glasses were analyzed for boron concentration by secondary ion mass spectrometry (SIMS) and for major elements and chlorine by electron microprobe. The composition of the coexisting fluid was calculated by mass balance. Boron partition coefficients between aqueous vapor and hydrous granitic melt range from 3.1 to 6.3, and demonstrate a clear preference of boron for the vapor over the hydrous melt. Partition coefficients between brine and hydrous granitic melt vary from 0.45 to 1.1, suggesting that boron has no preference for the brine or the melt. The bulk fluid–melt partition coefficients for low-salinity and high-salinity experiments are DB(vapor/melt)=4.6±1.3 and DB(brine/melt)=0.91±0.49, respectively. The corresponding vapor–brine partition coefficient is 5.0±3.1, demonstrating that boron partitions preferentially into the vapor over the brine at the conditions of this study. The preferential incorporation of boron in the aqueous vapor is controlled by borate speciation and solution mechanism. The dominant borate species in aqueous fluids, H3BO3o, is highly soluble in aqueous vapor (XB2O3=0.187); however, B2O3 is immiscible in NaCl liquid. Consequently, concentrations of boron in aqueous vapor are significantly higher than in the coexisting brine. Furthermore, Na–B complexing in the melt at high chlorine fluid contents stabilizes boron in the melt thereby contributing to the non-preferential partitioning of boron between brine and melt. The commonly observed association of tourmalinization (boron metasomatism), brecciation and ore deposition in nature is consistent with the preferential partitioning of boron into aqueous vapor of magmatic-hydrothermal systems predicted by this study.  相似文献   
33.
大别山碰撞后火山岩的锆石U-Pb年龄和氧同位素组成   总被引:11,自引:0,他引:11  
利用阴极发光技术 (CL)观察了大别山碰撞后玄武岩和安山岩的锆石内部结构 ,并通过离子探针技术 (SIMS)测定了其U Pb年龄和氧同位素组成。玄武岩中锆石都是直接从玄武质岩浆中结晶的岩浆锆石 ,其年龄为 130± 2Ma(1σ) ;安山岩中有两种锆石 ,绝大多数是直接从安山质岩浆中结晶出来的岩浆锆石 ,年龄为 133± 3Ma(1σ) ,少数是残留的原岩锆石 ,其年龄有两组 :76 8~80 5Ma和 182 7~ 1873Ma。玄武岩和安山岩的岩浆锆石年龄表明 ,大别山碰撞后火山岩的主体应形成于 130Ma左右 ,属早白垩世。结合文献资料来看 ,大别山碰撞后火山岩和侵入岩无论是化学组成、微量元素配分、Sr Nd同位素比值还是年龄 ,都是基本一致的 ,说明火山岩和侵入岩的源区以及成因可能是相同的。玄武岩和安山岩的岩浆结晶年龄一致 ,暗示着它们之间的可能的成因联系。玄武岩锆石相对于正常地幔亏损18O(δ18O =(4 .1± 0 .6 )‰ ) ,说明其岩浆源区可能含有一定数量的俯冲板块断离后进入该区地幔的大别山榴辉岩原岩组分。安山岩中残留的原岩锆石既有扬子板块的年龄信息 ,又有华北板块的年龄信息 ,这表明华北和扬子的深部界线可能就在北淮阳  相似文献   
34.
Secondary ion mass spectrometry (SIMS or ion microprobe) remains one of the most powerful tools available to the analytical geochemist. Despite the impressive progress witnessed by other competing laboratory methods over recent years, SIMS remains unsurpassed in its combination of small sampling volumes with low analytical uncertainties. Although the current SIMS analytical design has existed for over three decades, the period 2006–2007 saw significant advances in instrumentation, analytical methodology and, not least, the characterisation of new reference materials upon which all analyses depend. As of the end of 2007 the SIMS geoscience literature was reporting total sampling masses down to the 10 fg range, spatial resolution of better than 100 nm and uncertainties on major element isotope ratio determinations of better than ± 0.2‰ (1s). This article intends to synthesise the progress made by the geo‐SIMS community during this two year period and will also highlight some specific research results that were only possible due to the unique capabilities provided by SIMS.  相似文献   
35.
《地学前缘(英文版)》2020,11(5):1593-1608
The Gejiu-Bozushan-Laojunshan W-Sn polymetallic metallogenic belt(GBLB) in southeast Yunnan Province is an important part of the southwestern Yangtze Block in South China.Tin polymetallic mineralization in this belt includes the Niusipo,Malage,Songshujiao,Laochang and Kafang ore fields in the Gejiu area which are spatially and temporally associated with the Kafang-Laochang and Songshujiao granite plutons.These granites are characterized by variable A/CNK values(mostly 1.1,except for two samples with 1.09),high contents of SiO_2(74.38-76.84 wt.%) and Al_2 O_3(12.46-14.05 wt.%) and variable CaO/Na_2 O ratios(0.2-0.65) as well as high zircon δ~(18)O values(7.74‰-9.86‰),indicative of S-type affinities.These rocks are depleted in Rb,Th,U,Ti,LREE[(La/Yb)N=1.4-20.51],Ba,Nb,Sr,and Ti and display strong negative Eu and Ba anomalies.The rocks possess high Rb/Sr and Rb/Ba ratios,relatively low initial ~(87)Sr/~(86)Sr ratios(0.6917-0.7101),and less radiogenic εNd(t)values(-8.0 to-9.1).The zircon grains from these rocks show negative ε_(Hf)(t) values in the range of-3.7 to-9.9 with mean T_(DM2)(Nd) and T_(DM2)(Hf) values of 1.57 Ga and 1.55 Ga.They show initial ~(207)Pb/~(204)Pb ranging from15.69 to 15.71 and ~(206)Pb/~(204)Pb from 18.36 to 18.70.Monazite from Songshujiao granites exhibits higher U and lower Th/U ratios,lower δ~(18)O values and higher ε_(Hf)(t) values than those of the zircon grains in the KafangLaochang granites.The geochemical and isotopic features indicate that the Laochang-Kafang granites originated by partial melting of Mesoproterozoic crustal components including biotite-rich metapelite and metagraywacke,whereas the Songshujiao granites were derived from Mesoproterozoic muscovite-rich metapelite crustal source.Most zircon grains from the Songshujiao,Laochang and Kafang granites have high-U concentrations and their SIMS U-Pb ages show age scatter from 81.6 Ma to 88.6 Ma,80.7 Ma to 86.1 Ma and 82.3 Ma to 87.0 Ma,suggesting formation earlier than the monazite and cassiterite.Monazite SIMS U-Pb ages and Th-Pb ages of three same granite samples are consistent and show yielded 206 Pb/~(238)U ages of 83.7 ± 0.6 Ma,83.7±0.6 Ma,and 83.4±0.6 Ma,and ~(208)Pb/~(232)Th ages of 83.2 ± 0.5 Ma,83.8 ± 0.4 Ma,and 83.5±0.9 Ma,which are within the range of the SIMS zircon U-Pb ages from these rocks.The data constrain the crystallization of the granites at ca.83 Ma.In situ U-Pb dating of two cassiterite samples from the cassiterite-sulfide ore in the Songshujiao ore field and Kafang ore field,and two from the cassiterite-oxide+cassiterite bearing dolomite in the Laochang ore field yielded weighted mean 206 Pb/~(238)U ages of 83.5±0.4 Ma(MSWD=0.6),83.5 ± 0.4 Ma(MSWD=0.5),83.6 ±0.4 Ma(MSWD=0.6) and 83.2 ±0.7 Ma(MSWD=0.6),respectively.Combined with geological characteristics,the new geochronological data indicate that the formation of the granites and Sn polymetallic deposits are coeval.We correlate the magmatic and metallogenic event with lithospheric thinning and asthenosphere upwelling in continental extension setting in relation to the eastward subduction of the Neo-Tethys beneath the Sanjiang tectonic domain during Late Cretaceous.  相似文献   
36.
Aluminium tracer diffusivities were measured in polycrystalline mullite. The artificial aluminium isotope 26Al was used as tracer isotope. An advanced preparation technique for the 26Al2O3 tracer source allowed to apply secondary ion mass spectrometry (SIMS) in order to analyse 26Al depth distributions in the polycrystalline material. Pre-exponential factors and activation enthalpies were determined for compositions of 78 wt.% Al2O3, 22 wt.% SiO2 (high-alumina material) and of 72 wt.% Al2O3, 28 wt.% SiO2 (low-alumina material), respectively. A strong dependence of the 26Al grain boundary diffusivity on the composition is observed. The results are discussed in comparison to previous data on grain boundary diffusivities of oxygen in mullite samples from the same batch. Dedicated to Prof. Hermann Schmalzried on the occasion of his 75th birthday.  相似文献   
37.
Glass inclusions in plagioclase and orthopyroxene from daciticpumice of the Cabrits Dome, Plat Pays Volcanic Complex in southernDominica reveal a complexity of element behavior and Li–Bisotope variations in a single volcanic center that would gounnoticed in a whole-rock study. Inclusions and matrix glassesare high-silica rhyolite with compositions consistent with about50% fractional crystallization of the observed phenocrysts.Estimated crystallization conditions are 760–880°C,200 MPa and oxygen fugacity of FMQ + 1 to +2 log units (whereFMQ is the fayalite–magnetite–quartz buffer). Manyinclusion glasses are volatile-rich (up to 6 wt % H2O and 2900ppm Cl), but contents range down to 1 wt % H2O and 2000 ppmCl as a result of shallow-level degassing. Sulfur contents arelow throughout, with <350 ppm S. The trace element compositionof inclusion glasses shows enrichment in light rare earth elements(LREE; (La/Sm)n = 2·5–6·6) and elevatedBa, Th and K contents compared with whole rocks and similaror lower Nb and heavy REE (HREE; (Gd/Yb)n = 0·5–1·0).Lithium and boron concentrations and isotope ratios in meltinclusions are highly variable (20–60 ppm Li with 7Li= +4 to +15 ± 2; 60–100 ppm B with 11B = +6 to+13 ± 2) and imply trapping of isotopically heterogeneous,hybrid melts. Multiple sources and processes are required toexplain these features. The mid-ocean ridge basalt (MORB)-likeHREE, Nb and Y signature reflects the parental magma(s) derivedfrom the mantle wedge. Positive Ba/Nb, B/Nb and Th/Nb correlationsin inclusion glasses indicate coupled enrichment in stronglyfluid-mobile (Ba, B) and less-mobile (Th, Nb) trace elements,which can be explained by fractional crystallization of plagioclase,orthopyroxene and Fe–Ti oxides. The 7Li and 11B valuesare at the high end of known ranges for other island arc magmas.We attribute the high values to a 11B and 7Li-enriched slabcomponent derived from sea-floor-altered oceanic crust and possiblyfurther enriched in heavy isotopes by dehydration fractionation.The heterogeneity of isotope ratios in the evolved, trappedmelts is attributed to shallow-level assimilation of older volcanicrocks of the Plat Pays Volcanic Complex. KEY WORDS: subduction; volcanic arcs; igneous processes; melt inclusions; SIMS; trace elements; lithium and boron isotopes; diffusion  相似文献   
38.
The Variscan orogenesis in Europe peaked during the Late Devonian–Early Carboniferous times when Gondwanan terranes collided with Laurasia. Hitherto it has been thought that Carboniferous tectonics in northern Arabia and the adjacent parts of NE Africa were broad swells (‘arches’) and depressions (‘basins’) that formed as a far-field contractional effect of the Variscan compression. The discovery of a 351 ± 3 Ma (U–Pb in zircon) within-plate felsic volcanism in the Helez borehole, southern coastal Israel, suggests that the Levant Arch is, instead, extensional in origin. Felsic volcanism was associated with gabbro underplating of the crust, an extreme (~50°C/km) crustal thermal gradient, major uplift, and truncation of the ≥2.5 km section. Taken together with the recent discovery of the ~340 Ma oceanic crust in the Eastern Mediterranean, the Levant Arch is interpreted as an uplifted shoulder of a rift, preceding ocean spreading.  相似文献   
39.
范宏瑞  李兴辉  左亚彬  陈蕾  刘尚  胡芳芳  冯凯 《岩石学报》2018,34(12):3479-3496
硫化物微区原位分析技术包括LA-ICPMS定点微量元素分析、LA-ICPMS和(Nano) SIMS微量元素面扫描分析,以及SIMS、Nano SIMS和LA-MC-ICPMS原位硫同位素点分析和面扫描。这些分析方法可以有效地获取不同期次硫化物微量元素含量、丰度分布图像、硫同位素比值和分布特征,结合微区时间分辨信号谱图、微量元素相关性分析等,在矿床学的成矿元素行为与赋存状态、成矿元素置换反应、成矿流体与硫的来源、矿石矿物的化学分带性、矿床成因模型等研究中有着重要的应用前景,以探讨矿床的精细成矿过程。硫化物原位微量元素和同位素LA-(MC)-ICPMS和(Nano) SIMS分析,需要降低仪器和分析方法的系统误差,克服严重的基体效应和同位素分馏效应。  相似文献   
40.
《Resource Geology》2018,68(1):1-21
The Daheishan Mo deposit of the Lesser Xing'an–Zhangguangcai Range metallogenic belt in northeast China is a super‐large molybdenum deposit with Mo reserves of 1.09 Mt. The Mo mineralization occurs mainly in a granodiorite porphyry. Zircon SIMS U–Pb dating yields a crystallization age of 168.3 ± 1.4 Ma for the granodiorite porphyry. Molybdenite Re–Os dating indicates that Mo mineralization occurred at 169.2 ± 1.2 Ma. These geochronological data indicate that these magmatic and hydrothermal activities occurred during the Middle Jurassic. The granodiorite porphyry can be classified as high‐K calc‐alkaline series, and the rare earth elements (REE) are characterized by a significant fractionation between light REE (LREE) and heavy REE (HREE) with slightly positive Eu anomalies (Eu/Eu* = 1.08–1.12). Large ion lithophile elements (e.g., Rb, U, K, and Pb) are enriched, whereas high field strength elements (e.g., Nb, Ta, Ti, HREEs, and Yb) are strongly depleted. The granodiorite porphyry is also characterized by initial strontium isotope ratios (87Sr/86Sr)i of 0.70460–0.70482 and magmatic zircon δ18O values of 5.2–6.5 ‰ that are similar to those of the mantle. Zircon ɛHf(t) and whole‐rock ε Nd(t) values range from 5.6 to 9.9 and 0.8 to 1.1, respectively. The two‐stage Nd model ages (TDM2) are in the range of 868–894 Ma, similar to Hf model ages, indicating that the parent magma has a uniform source and primarily originated from a juvenile crustal source. Combined with the regional geological history, geochemistry of the Daheishan granodiorite porphyry, and new isotopic age data, we propose that the formation of the Daheishan porphyry Mo deposit is likely related to the subduction of the Paleo‐Pacific Plate.  相似文献   
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